医療従事者の為の最新医療ニュースや様々な情報・ツールを提供する医療総合サイト

Sapient Therapeutics Announces Positive Phase 1 Results in Part B of Its Solid Dose Prescription CBD Study

2023年12月19日 PM09:00
このエントリーをはてなブックマークに追加


 

LONDON & MELBOURNE, Australia

Sapient Therapeutics Ltd (“Sapient Therapeutics”), a pioneering biopharmaceutical company specialising in neuroscience drug discovery and early clinical development, is pleased to announce the successful completion of Part B of its Phase 1 comparative trial evaluating the safety and pharmacokinetics of its innovative solid dose prescription cannabidiol (CBD), SAP021.

The positive results of this two-part Phase 1 trial demonstrate the tolerability and bioavailability of Sapient Therapeutics’ lead asset, SAP021, in comparison to Epidiolex®. The trial met all pharmacokinetic objectives, marking a significant milestone in the development of SAP021. As a result, the Company will be progressing this solid dose prescription-only CBD candidate into further clinical development and will meet with the U.S. Regulatory Authorities (Food and Drug Administration, FDA) at a Pre-IND meeting in H1 2024

Giles Moss, Chief Executive Officer of Sapient Therapeutics commented: “The success of Part B of our Phase 1 study confirms the promise for SAP021. When SAP021 was given with food the data were in alignment with both our expectations from Part A of the study and with previously published trial results. We now look forward to the next stage of clinical development. We would like to express our gratitude to all the volunteers and trial staff for their contribution to this successful result.” Sapient Therapeutics plans to utilise the FDA 505(b)(2) expedited regulatory pathway, with a view to making a solid dose CBD prescription medicine commercially available for US patients in the shortest possible timeframe.

For and on behalf of Sapient Therapeutics Ltd:

Sapient Therapeutics is a UK based biopharmaceutical company focused on neuroscience drug discovery and early clinical development. Our lead asset (SAP021) has successfully completed its first Phase 1 study with the Clinical Study Report (CSR) expected in H1 2024. Our leadership team is comprised of neuroscience and cannabinoid medicine veterans. Together we are utilising the experience gained in cannabinoid drug development to bring new prescription medicines to patients suffering from serious diseases.

Code: STx PR002, Date of preparation: Dec2023

View source version on businesswire.com: https://www.businesswire.com/news/home/20231219320924/en/

CONTACT

Giles Moss, CEO

gmoss@sapienttx.com

同じカテゴリーの記事 

  • Ifinatamab Deruxtecan Continues to Demonstrate Promising Objective Response Rates in Patients with Extensive-Stage Small Cell Lung Cancer in IDeate-Lung01 Phase 2 Trial
  • Huonslab Announces Positive Results from In Vivo comparative PK study of Trastuzumab/HyDIFFUZETM compared with marketed rHuPH20 co-formulation with Trastuzumab
  • Rapid Medical™、TIGERTRIEVER™13を用いたDISTALS臨床試験の中間安全性解析で、中血管閉塞の安全性の懸念がないことを報告
  • Amneal and Shilpa Announce U.S. FDA Approval of BORUZU™, the First Ready-to-Use Version of Bortezomib for subcutaneous administration
  • JCR Pharmaceuticals’ Data Presentations at SSIEM Annual Symposium 2024 Highlight Investigational Treatments for Lysosomal Storage Disorders